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Biocompatibility Manager Jobs in Virginia (NOW HIRING)

Luna Labs USA

Cell Biologist

Charlottesville, VA

$70K - $90K/yr

... biocompatibility and safety of biomaterial prototypes. * Instrumentation Management: Maintain, calibrate, and operate laboratory instrumentation and equipment to ensure reliable performance and data ...

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Biocompatibility Manager information

What are the key skills and qualifications needed to thrive as a biocompatibility manager?

To thrive as a Biocompatibility Manager, you need expertise in toxicology, materials science, and regulatory standards, typically supported by a degree in a life science field and experience with medical device biocompatibility testing. Familiarity with ISO 10993 standards, risk assessment tools, and regulatory submission systems is essential. Strong analytical thinking, attention to detail, and effective communication skills help in collaborating with cross-functional teams and ensuring regulatory compliance. These skills and qualities are vital for ensuring product safety, regulatory approval, and successful market entry for medical devices.

What are the common challenges a biocompatibility manager faces when coordinating cross-functional teams during product development?

A Biocompatibility Manager often encounters challenges in aligning the priorities and timelines of various teams such as R&D, regulatory affairs, and quality assurance. Ensuring clear communication about testing requirements and regulatory updates is vital, as misunderstandings can lead to delays or non-compliance issues. Additionally, the manager must balance thorough risk assessments with project deadlines, all while staying current with evolving international standards. Effective collaboration and proactive problem-solving are key to overcoming these challenges and ensuring the safety and compliance of medical devices.

What does a biocompatibility manager do?

A Biocompatibility Manager oversees the evaluation and testing of medical devices and materials to ensure they are safe and compatible with human tissues. Their responsibilities include designing testing protocols, interpreting regulatory requirements, and ensuring compliance with international standards like ISO 10993. They work closely with research, development, and regulatory teams to address any risks related to biological safety. Their work is critical for gaining regulatory approvals and ensuring patient safety.

What is the difference between Biocompatibility Manager vs Biocompatibility Specialist?

AspectBiocompatibility ManagerBiocompatibility Specialist
CredentialsTypically requires a degree in life sciences or biomedical engineering; certifications like ISO 10993 are commonSimilar educational background; often holds certifications in biocompatibility testing
Work EnvironmentOversees teams, manages projects, and ensures compliance across departmentsPerforms testing, data analysis, and reports within labs or R&D settings
Industry UsageUsed in regulatory, quality assurance, and management roles within medical device companiesPrimarily involved in testing and technical analysis within laboratories

The main difference is that the Biocompatibility Manager oversees testing programs and compliance strategies, while the Biocompatibility Specialist focuses on conducting tests and technical analysis. Both roles require similar credentials but differ in scope and responsibilities.

What are the most commonly searched types of Biocompatibility jobs in Virginia? The most popular types of Biocompatibility jobs in Virginia are:
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Biocompatibility Manager jobs near you
Infographic showing various Biocompatibility Manager job openings in Virginia as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 89% In-person, and 11% Remote job distribution.

Senior Engineer

Weinert Fiber Optics, Inc.

Williamsburg, VA • On-site

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

About the Role:

As an Engineer you will play a critical role in the design, development, and manufacturing of high-precision fiber optic components used in industrial and medical devices. You will collaborate closely with cross-functional teams including engineering, quality assurance, and production to optimize assembly processes and troubleshoot technical challenges. This role demands a broad engineering skillset to drive manufacturing best practices with the goal of delivering assemblies that meet stringent customer and regulatory requirements.


Responsibilities:

  • Design and develop fiber optic assemblies tailored for specific, highly stringent applications, ensuring compliance with industry standards and regulatory requirements.
  • Collaborate with manufacturing teams to establish and refine assembly processes that maximize efficiency, yield, and product quality.
  • Perform detailed testing and validation documentation of fiber optic assemblies to verify performance specifications and reliability under application use conditions.
  • Analyze and resolve technical issues related to fiber optic components and assemblies, providing engineering support throughout the product lifecycle.
  • Document engineering activities, including design changes, test results, validations, and process improvements, maintaining thorough records for regulatory compliance.
  • Work closely with suppliers and vendors to source high-quality materials and components.
  • Participate in continuous improvement initiatives to enhance product design, reduce costs, and accelerate time-to-market.


Minimum Qualifications:

  • Bachelor’s degree in Engineering, or a related technical field.
  • Familiarity with medical, industrial, and/or aerospace device manufacturing standards such as ISO9001, AS9100, ISO13485 and FDA standards.
  • Proficient in validation of medical, industrial, and aerospace processes, equipment, and components.
  • Working knowledge of managing a design and development process in a highly regulated industry.
  • Strong problem-solving skills with the ability to analyze complex technical issues and implement effective solutions.
  • Experience working in a regulated medical device, aerospace, and/or semiconductor manufacturing environment.
  • Eligible to legally work in the United States of America
  • Must be a U.S. Person as defined by 22 C.F.R. § 120.62


Preferred Qualifications:

  • Master’s degree in a relevant engineering discipline.
  • Experience in fiber optics technology, particularly in assembly, testing, or design of fiber optic components.
  • Understanding of biocompatibility and sterilization processes related to medical device assemblies.
  • Knowledge of cleanroom standards and practices.


What We Offer:

  • The pay range for this salaried position is $80,000 -$120,000 annually including a target incentive.
  • Benefits include healthcare insurance including dental, vision, HSA, and life insurance.
  • WEINERT offers a 401 (k) retirement plan with a 100% company match up to 4% of salary.